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D C Bittel

Showing results (1-10 of 13) with videos related to

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TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 9, 2013
Dosage response of rye genes in a wheat background : 2. Secalin genes on 1RSD C Bittel, J P Gustafson
The Journal of Biological Chemistry|August 26, 2000
Functional heterogeneity in the zinc fingers of metalloregulatory protein metal response element-binding transcription factor-1D C Bittel, I V Smirnova, G K Andrews
American Journal of Medical Genetics. Part A|August 14, 2008
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) arrayH L Newkirk, D C Bittel, M G Butler
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 30, 2013
Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthaseD C Bittel, J M Shaver, D A Somers, et al.
The Journal of Biological Chemistry|March 29, 2000
Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1I V Smirnova, D C Bittel, R Ravindra, et al.
Journal of Autism and Developmental Disorders|September 17, 2005
Brief report: non-random X chromosome inactivation in females with autismZ Talebizadeh, D C Bittel, O J Veatch, et al.
International Journal of Obesity (2005)|October 19, 2005
Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjectsL Kennedy, D C Bittel, N Kibiryeva, et al.
Journal of Medical Genetics|December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human femalesD C Bittel, M F Theodoro, N Kibiryeva, et al.
Cytogenetic and Genome Research|May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGHD C Bittel, S Yu, H Newkirk, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 9, 2013
Dosage response of rye genes in a wheat background : 2. Secalin genes on 1RSD C Bittel, J P Gustafson
The Journal of Biological Chemistry|August 26, 2000
Functional heterogeneity in the zinc fingers of metalloregulatory protein metal response element-binding transcription factor-1D C Bittel, I V Smirnova, G K Andrews
American Journal of Medical Genetics. Part A|August 14, 2008
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) arrayH L Newkirk, D C Bittel, M G Butler
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 30, 2013
Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthaseD C Bittel, J M Shaver, D A Somers, et al.
The Journal of Biological Chemistry|March 29, 2000
Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1I V Smirnova, D C Bittel, R Ravindra, et al.
Journal of Autism and Developmental Disorders|September 17, 2005
Brief report: non-random X chromosome inactivation in females with autismZ Talebizadeh, D C Bittel, O J Veatch, et al.
International Journal of Obesity (2005)|October 19, 2005
Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjectsL Kennedy, D C Bittel, N Kibiryeva, et al.
Journal of Medical Genetics|December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human femalesD C Bittel, M F Theodoro, N Kibiryeva, et al.
Cytogenetic and Genome Research|May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGHD C Bittel, S Yu, H Newkirk, et al.
Pageof 2